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dc.contributor.authorChen, K.
dc.contributor.authorLiu, S.
dc.contributor.authorAi, N.
dc.contributor.authorKoyama, M.
dc.contributor.authorJiang, San Ping
dc.date.accessioned2017-01-30T13:48:48Z
dc.date.available2017-01-30T13:48:48Z
dc.date.created2016-02-01T00:47:09Z
dc.date.issued2015
dc.identifier.citationChen, K. and Liu, S. and Ai, N. and Koyama, M. and Jiang, S.P. 2015. Why solid oxide cells can be reversibly operated in solid oxide electrolysis cell and fuel cell modes? Physical Chemistry Chemical Physics. 17 (46): pp. 31308-31315.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/35288
dc.identifier.doi10.1039/c5cp05065k
dc.description.abstract

© 2015 the Owner Societies. High temperature solid oxide cells (SOCs) are attractive for storage and regeneration of renewable energy by operating reversibly in solid oxide electrolysis cell (SOEC) and solid oxide fuel cell (SOFC) modes. However, the stability of SOCs, particularly the deterioration of the performance of oxygen electrodes in the SOEC operation mode, is the most critical issue in the development of high performance and durable SOCs. In this study, we investigate in detail the electrochemical activity and stability of La0.8Sr0.2MnO3 (LSM) oxygen electrodes in cyclic SOEC and SOFC modes. The results show that the deterioration of LSM oxygen electrodes caused by anodic polarization can be partially or completely recovered by subsequent cathodic polarization. Using in situ assembled LSM electrodes without pre-sintering, we demonstrate that the deteriorated LSM/YSZ interface can be repaired and regenerated by operating the cells under cathodic polarization conditions. This study for the first time establishes the foundation for the development of truly reversible and stable SOCs for hydrogen fuel production and electricity generation in cyclic SOEC and SOFC operation modes.

dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/DP150102025
dc.titleWhy solid oxide cells can be reversibly operated in solid oxide electrolysis cell and fuel cell modes?
dc.typeJournal Article
dcterms.source.volume17
dcterms.source.number46
dcterms.source.startPage31308
dcterms.source.endPage31315
dcterms.source.issn1463-9076
dcterms.source.titlePhysical Chemistry Chemical Physics
curtin.departmentFuels and Energy Technology Institute
curtin.accessStatusFulltext not available


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